Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Poly(polyoxotungstate)s with 20 Nickel Centers: From Nanoclusters to One-Dimensional Chains

2009

NickelCrystallographychemistryPolyoxometalateCluster (physics)chemistry.chemical_elementGeneral MedicineGeneral ChemistryPhotochemistryCatalysisNanoclustersAngewandte Chemie International Edition
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ChemInform Abstract: Merging Visible-Light-Photoredox and Nickel Catalysis

2015

Review: [scope and limitations of the combination of nickel and photoredox catalysis for Csp3—Csp2 cross-coupling reactions; 18 refs.

NickelScope (project management)chemistryPhotoredox catalysischemistry.chemical_elementGeneral MedicinePhotochemistryCatalysisVisible spectrumChemInform
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A tetranuclear organorhenium(i) complex of the 2,3,5,6-tetrafluoro-7,7,8,8-tetracyano-p-quinodimethane radical anion, TCNQF4˙−

2008

The radical complex {(mu(4)-TCNQF4)[Re(CO)(3)(bpy)](4)}(PF(6))(3), as prepared and isolated from the reaction between TCNQF4 and [Re(CO)(3)(bpy)(MeOH)](PF(6)), was studied electrochemically and by IR vibrational spectroscopy, UV-Vis-NIR absorption spectroscopy, and by EPR at 9.5, 190 and 285 GHz. The isotropic g factor of 2.0058, the detectable g anisotropy, and the (185,187)Re EPR hyperfine coupling of 0.95 mT for four equivalent metal nuclei support predominant, but not exclusive, spin localisation at the bridging ligand. Nitrile and metal carbonyl stretching frequencies as well as the typically structured near infrared absorption band lend further support to (TCNQF4 (-))(Re(I))(4) as the…

NitrileAbsorption spectroscopyChemistryLigandInfrared spectroscopyBridging ligandMetal carbonylPhotochemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundElectron transferCrystallographylawElectron paramagnetic resonanceDalton Transactions
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A DFT study of the role of Lewis acid catalysts in the mechanism of the 1,3-dipolar cycloaddition of nitrile imines towards electron-deficient acrylo…

2012

Abstract The role of the Mg complex formation in the reaction rate and regioselectivity of the 1,3-dipolar cycloaddition (13DC) reactions of nitrile imines (NIs) towards electron-deficient methacryloylpyrazolidinones has been theoretically studied using DFT methods at the B3LYP/6-31G * level. These 13DC reactions have an asynchronous concerted mechanism with a low polar character, displaying a high C regioselectivity induced by a steric repulsion between the phenyl substituent present at the C3 carbon of the NIs and the pyrazolidinone appendage present in the methacryloyl derivative, which increases with the formation of the bulky Mg–methacryloylpyrazolidinone complex. Solvent effect has be…

NitrileChemistryConcerted reactionRegioselectivityCondensed Matter PhysicsPhotochemistryBiochemistryPolarizable continuum modelMedicinal chemistryCycloadditionchemistry.chemical_compound13-Dipolar cycloadditionLewis acids and basesPhysical and Theoretical ChemistrySolvent effectsComputational and Theoretical Chemistry
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Phosphorescence emission and polarization of quinoline 3-carbonitrile

1993

Abstract The phosphorescence emission and excitation spectra and their polarization have been studied for quinoline 3-carbonitrile in methylcyclohexane and ethanol glasses at 77 K. From the results obtained in this molecule (τ=1.15 sec in ethanol, τ=1.04 sec in methylcyclohexane and out-of-plane polarization) it is concluded that the emission is orginated from a triplet state of 3 ππ * character. The two major spin-orbit coupling mechanisms through which the ππ * state of quinoline 3-carbonitrile acquires dipole-allowed character via nπ * states are: 1. In ethanol glass: 2. In methylcyclohexane glass:

NitrileOrganic ChemistryQuinolinePhotochemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryMoleculeEmission spectrumMethylcyclohexaneTriplet statePolarization (electrochemistry)PhosphorescenceSpectroscopyJournal of Molecular Structure
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Pyrene-functionalized nanoparticles: two independent sensors, the excimer and the monomer.

2012

The high surface-to-volume ratio of nanoparticles has been used to obtain a high local concentration of pyrene units on their periphery, making the formation of both pyrene emissive species possible using amazingly small pyrene concentrations. The sensing properties of model pyrene-functionalized nanoparticles was investigated by using different nitroaromatic compounds [m-nitroaniline and p-nitroaniline] and nitrobenzenes [nitrobenzene, p-nitrotoluene, 2,4-dinitrotoluene, and 2,6-dinitrotoluene]. The hybrid system acts as a dual-fluorescence sensor, in which the decrease of the pyrene emission, induced by the quencher, is hardly reflected in the pyrene excimer emission. The encapsulation ca…

NitrobenzeneAnalytechemistry.chemical_compoundMonomerFunctionalized nanoparticleschemistryNanoparticlePyreneExcimerPhotochemistryAnalytical ChemistryAnalytical chemistry
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Understanding the Mechanism of Nitrobenzene Nitration with Nitronium Ion: A Molecular Electron Density Theory Study

2019

Nitrobenzenechemistry.chemical_compoundElectron densitychemistryNitrationNitronium ionMolecular mechanismGeneral ChemistryElectrophilic aromatic substitutionPhotochemistryMechanism (sociology)ChemistrySelect
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Growth of polyoxymethylene crystals during cationic polymerization of trioxane in nitrobenzene

1973

Nitrobenzenechemistry.chemical_compoundTrioxanePolyoxymethyleneChemistryPolymer chemistryGeneral EngineeringCationic polymerizationGeneral Materials SciencePhotochemistryJournal of Polymer Science: Polymer Letters Edition
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Nitrogen and sulfur co-doped carbon nanodots toward bovine hemoglobin: A fluorescence quenching mechanism investigation

2018

A deep understanding of the molecular interactions of carbon nanodots with biomacromolecules is essential for wider applications of carbon nanodots both in vitro and in vivo. Herein, nitrogen and sulfur co-doped carbon dots (N,S-CDs) with a quantum yield of 16% were synthesized by a 1-step hydrothermal method. The N,S-CDs exhibited a good dispersion, with a graphite-like structure, along with the fluorescence lifetime of approximately 7.50 ns. Findings showed that the fluorescence of the N,S-CDs was effectively quenched by bovine hemoglobin as a result of the static fluorescence quenching. The mentioned quenching mechanism was investigated by the Stern-Volmer equation, temperature-dependent…

NitrogenQuantum yieldchemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciencesHemoglobinsStructural BiologyQuantum DotsAnimalsMolecular Biologybovine hemoglobinQuenching (fluorescence)010401 analytical chemistryFluorescenceSulfurAcceptorNitrogenCarbon0104 chemical sciencesquenching mechanismchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCattlefluorescenceDispersion (chemistry)CarbonSulfurnitrogen and sulfur co-doped carbon dotsJournal of Molecular Recognition
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How Hydrogen Bonds Affect Reactivity and Intervalence Charge Transfer in Ferrocenium‐Phenolate Radicals

2016

The ferrocenyl-phenol 2,4-di-tert-butyl-6-(ferrocenylcarbamoyl)phenol (H-1) forms intramolecular hydrogen bonds which are absent in its constitutional isomer 2,6-di-tert-butyl-4-(ferrocenylcarbamoyl)phenol (H-2). Their corresponding bases 1– and 2– show intra- and intermolecular NH···O hydrogen bonds, respectively. The phenolate 1– is reversibly oxidized to 1·, whereas 2– only undergoes a quasi-reversible oxidation to 2·, which suggests a higher reactivity. The radical pools of 1· and 2· formed by the oxidation/deprotonation of H-1 and H-2 have been probed by (rapid-freeze) electron paramagnetic resonance (EPR) spectroscopy and by spin-trapping techniques to elucidate the types of radicals …

Nitroxide mediated radical polymerization010405 organic chemistryChemistryHydrogen bondRadicalIntervalence charge transfer010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical scienceslaw.inventionInorganic ChemistryDeprotonationlawValence isomerIntramolecular forceElectron paramagnetic resonanceEuropean Journal of Inorganic Chemistry
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